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Variant : CV159016 (GRCh38/hg38 3q28(chr3:188491113-188671505)x1) Homo sapiens

Symbol: CV159016
Name: GRCh38/hg38 3q28(chr3:188491113-188671505)x1
Condition: See cases [RCV000138315]
Clinical Significance: uncertain significance
Last Evaluated: 06/01/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LPP   LPP-AS1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_188491113)_(188671505_?)del
NC_000003.11:g.(?_188208901)_(188389293_?)del
NC_000003.10:g.(?_189691595)_(189871987_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh383188,491,113 - 188,671,505CLINVAR
GRCh373188,208,901 - 188,389,293CLINVAR
Build 363189,691,595 - 189,871,987CLINVAR
Cytogenetic Map33q28CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485864
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-07
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.